Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Maria Khoueiry"'
Publikováno v:
Case Reports in Neurological Medicine, Vol 2021 (2021)
Introduction. Spinal neurosarcoidosis is a rare disease that can manifest as myelopathy, radiculopathy, or cauda equine syndrome. Spinal epidural lipomatosis is also a rare condition resulting from overgrowth of epidural fat tissue causing compressiv
Externí odkaz:
https://doaj.org/article/1c021c00b8f647d28d2b55b150f20259
Autor:
Halim Tannous, Shadi Akiki, Rasha E. Boulos, Charlene El Khoury Eid, Ghadi El Hasbani, Lea Maria Khoueiry, Lynn El Khoury, Rawan Tohme, Rim Moussa, Georges Khazen
Publikováno v:
BMC Infectious Diseases, Vol 22, Iss 1, Pp 1-7 (2022)
Abstract The world has been dealing with the SARS-COV-2 pandemic since December 2019 and a lot of effort has focused on tracking the spread of the virus by gathering information regarding testing statistics and generating viral genomic sequences. Unf
Externí odkaz:
https://doaj.org/article/9671fa0783f143a085414c8496e82b57
Autor:
Lynn El Khoury, Shadi Akiki, Rim Moussa, Lea Maria Khoueiry, Ghadi El Hasbani, Rasha E. Boulos, Georges Khazen, Rawan Tohme, Charlene El Khoury Eid, Halim Tannous
Publikováno v:
BMC Infectious Diseases. 22
The world has been dealing with the SARS-COV-2 pandemic since December 2019 and a lot of effort has focused on tracking the spread of the virus by gathering information regarding testing statistics and generating viral genomic sequences. Unfortunatel
Publikováno v:
Lebanese Medical Journal. 69:46-48
Publikováno v:
Case Reports in Neurological Medicine
Case Reports in Neurological Medicine, Vol 2021 (2021)
Case Reports in Neurological Medicine, Vol 2021 (2021)
Introduction. Spinal neurosarcoidosis is a rare disease that can manifest as myelopathy, radiculopathy, or cauda equine syndrome. Spinal epidural lipomatosis is also a rare condition resulting from overgrowth of epidural fat tissue causing compressiv
Publikováno v:
J Spinal Cord Med
Context: Non-traumatic spinal cord infarction in the young adult is usually associated with a single or multiple genetic mutations. There are certain gene mutations that are more commonly associated with spinal cord infarctions. Homozygous or heteroz
Publikováno v:
Amyotrophic lateral sclerosisfrontotemporal degeneration. 21(1-2)
Sandhoff disease is an under-recognized disease that may present as a lower motor neuron disorder in adulthood. We report the case of siblings presenting in their late 40s with a motor neuron disease phenotype and were misdiagnosed as amyotrophic lat
Autor:
Jean Mattar, Joseph Mattar, Elsa Mhanna, Anthony Eid, Maria Khoueiry, Elias Hajj, Kamal Kallab
Publikováno v:
Revue Neurologique. 174:S141-S142
Introduction Les traumatismes crâniens presentent un taux de morbidite et mortalite important. La severite du traumatisme et l’etat general du patient, ainsi que l’apparition de crises convulsives renvoient a des prises en charge controversees.
Publikováno v:
Revue Neurologique. 173:S171
Introduction L’inflammation est precoce dans la pathogenese des AVC (accident vasculaire cerebral) ischemiques. La CRP (C-reactive protein) est un marqueur pronostique et predictif de recurrence potentiel, mais les donnees dans l’AVC ischemique s